Glenmark Pharmaceuticals Limited Walk In Interview 2022.Glenmark Pharmaceuticals Limited Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.Glenmark Pharmaceuticals Limited [Glenmark] is an India-based growing pharmaceutical company headquartered at Mumbai [formerly, Bombay]. Incorporated in 1977, the Company is focused on the manufacture and marketing of formulation products and active pharmaceutical ingredients [API] in India as well as globally and enjoys a diversified and growing presence in regulated and developing international markets. Over the past five years, the Company has also catalysed its growth through investment in dedicated research and development including cutting-edge New Chemical Entity [NCE] research.
Vacancy details:
- Post Name: Site Investigation Lead
- Qualification: M.Pharma in Pharmacy, MS/M.Sc(Science) in Any Specialization
- Experienced:15 to 18 years
Job Description: Greeting from Glenmark Pharmaceuticals Limited !!!!
Important Details :
- Location: Aurangabad
- Post of date:07/12/2022
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Fact to face Interview
- Rounds of Interview: HR
Roles and Responsibilities :
1. To have knowledge on Product Development, QC lab operations, identification of CPPs and CQAs and evaluation of in-process, finished product and stability samples.
2. Have hands on experience of manufacturing operation of OSD, SSD formulation equipment and /or QC lab operations and sophisticated techniques.
3. Handling of QMS documents like. Incident / Deviation investigation, change control etc.
4. Have knowledge of electronic data management of manufacturing system and lab system
5. Review of QMS documents such as OOS, OOT, Incidents Deviation, CAPA, and product market complaint,
6. Have good understanding of statistical evaluation of data.
7. Performing root cause analysis of an occurred OOS, deviation / a typical event or Failure investigation using investigation tools viz. Fishbone diagram, 5 WHY Analysis, IS IS NOT Analysis, Peeling the Onion, Process Mapping / Flow Charts, Interviews and Brain Storming.
8. Reviewing the adequacy of CAPAs with respect to the root cause investigations. To verify if the CAPA EC is well defined.
9. Responding to internal as well as external audit observations with respect to investigation related observations.
10.To be able to identify and notify atypical product trends while review of investigations.
Desired Candidate Profile
Only relevant candidates with pharma background will be preferred. Kindly share updated resumes on prachi.jain1@glenmarkpharma.com with subject line “Application for SITL – Aurangabad”.
